Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5206014 | 6424719 | I | 5206014-6 | 20070103 | 20070108 | EXP | GBWYE012203JAN07 | WYETH PHARMACEUTICALS INC. | M | N | 20070105 | OT | UNITED KINGDOM |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
5206014 | 1008032731 | PS | EFFEXOR | 1 | ORAL | 150MG, FREQUENCY UNKNOWN, ORAL, 75 MG, FREQUENCY UNKNOWN | D | D | 20151 | ||
5206014 | 1008070765 | SS | MODAFINIL | 1 | ORAL | SEE IMAGE | D | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5206014 | 1008032731 | HYPERSOMNIA |
5206014 | 1008070765 | SLEEP APNOEA SYNDROME |
Outcome of event
Event ID | OUTC COD |
---|---|
5206014 | OT |
Reactions reported
Event ID | PT |
---|---|
5206014 | DRUG INTERACTION |
5206014 | DRUG WITHDRAWAL SYNDROME |
5206014 | PSYCHOTIC DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5206014 | FGN |
5206014 | HP |
5206014 | OTH |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5206014 | 1008070765 | 4 | WK |